2,6-bis(triphenylsilyl)-4,4-dimethylcyclopenta[2,1-b:3,4-b']dithiophene | 1314116-07-8

• 分子结构分类: 有机化合物 - 有机杂环化合物 - 噻吩类
• 英文名称: 2,6-bis(triphenylsilyl)-4,4-dimethylcyclopenta[2,1-b:3,4-b']dithiophene
• 英文别名: (7,7-Dimethyl-10-triphenylsilyl-3,11-dithiatricyclo[6.3.0.02,6]undeca-1(8),2(6),4,9-tetraen-4-yl)-triphenylsilane；(7,7-dimethyl-10-triphenylsilyl-3,11-dithiatricyclo[6.3.0.02,6]undeca-1(8),2(6),4,9-tetraen-4-yl)-triphenylsilane
• CAS: 1314116-07-8
• 化学式: C₄₇H₃₈S₂Si₂
• 分子量: 723.122
• InChiKey: ICKPYNBABOBCIF-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  6.87
• 重原子数：
  51
• 可旋转键数：
  8
• 环数：
  9.0
• sp3杂化的碳原子比例：
  0.06
• 拓扑面积：
  56.5
• 氢给体数：
  0
• 氢受体数：
  2

反应信息

• 作为产物：
  描述：

  4,4-dimethyl-4H-cyclopenta[1,2-b:5,4-b']dithiophene 在 N-溴代丁二酰亚胺(NBS) 、 正丁基锂 、 四甲基乙二胺 作用下， 以 乙醚 、 正己烷 、 N,N-二甲基甲酰胺 为溶剂， 反应 38.0h， 生成 2,6-bis(triphenylsilyl)-4,4-dimethylcyclopenta[2,1-b:3,4-b']dithiophene
  参考文献：
  名称：

  Fluorescent cyclopentadithiophene derivatives having phenyl-substituted silyl moieties

  摘要：

  4,4-Dimethylcyclopenta[2,1-b:3,4-b']dithiophene derivatives bearing trimethyl-, dimethylphenyl-, diphenylmethyl-, or triphenyl-silyl moieties were synthesized. The introduction of the silyl moieties onto cyclopenta[2,1-b:3,4-b']dithiophene induced fluorescent emission as well as the bathochromic shift of wavelength at the maximum absorption and fluorescence. It was found that the larger number of phenyl group on silyl moiety resulted in the higher fluorescence quantum yield. (C) 2011 Elsevier Ltd. All rights reserved.

  DOI：

  10.1016/j.tetlet.2011.05.128

文献信息

• Fluorescent cyclopentadithiophene derivatives having phenyl-substituted silyl moieties
  作者：Hitoshi Hanamura、Ryoko Haneishi、Nobukatsu Nemoto

  DOI：10.1016/j.tetlet.2011.05.128

  日期：2011.8

  4,4-Dimethylcyclopenta[2,1-b:3,4-b']dithiophene derivatives bearing trimethyl-, dimethylphenyl-, diphenylmethyl-, or triphenyl-silyl moieties were synthesized. The introduction of the silyl moieties onto cyclopenta[2,1-b:3,4-b']dithiophene induced fluorescent emission as well as the bathochromic shift of wavelength at the maximum absorption and fluorescence. It was found that the larger number of phenyl group on silyl moiety resulted in the higher fluorescence quantum yield. (C) 2011 Elsevier Ltd. All rights reserved.